Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Wolfe, Kate"'
Autor:
Wolfe, Kate1 k.wolfe@ucl.ac.uk, Stueber, Kerstin1, McQuillin, Andrew1, Jichi, Fatima2, Patch, Christine3, Flinter, Frances3, Strydom, André1, Bass, Nick1
Publikováno v:
Journal of Applied Research in Intellectual Disabilities. Mar2018, Vol. 31 Issue 2, p273-284. 12p.
Autor:
Wolfe, Kate, McQuillin, Andrew, Alesi, Viola, Boudry Labis, Elise, Cutajar, Peter, Dallapiccola, Bruno, Dentici, Maria Lisa, Dieux-Coeslier, Anne, Duban-Bedu, Benedicte, Duelund Hjortshøj, Tina, Goel, Himanshu, Loddo, Sara, Morrogh, Deborah, Mosca-Boidron, Anne-Laure, Novelli, Antonio, Olivier-Faivre, Laurence, Parker, Jennifer, Parker, Michael J, Patch, Christine, Pelling, Anna L, Smol, Thomas, Tümer, Zeynep, Vanakker, Olivier, van Haeringen, Arie, Vanlerberghe, Clémence, Strydom, Andre, Skuse, David, Bass, Nick
Publikováno v:
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
Wolfe, K, McQuillin, A, Alesi, V, Boudry Labis, E, Cutajar, P, Dallapiccola, B, Dentici, M L, Dieux-Coeslier, A, Duban-Bedu, B, Duelund Hjortshøj, T, Goel, H, Loddo, S, Morrogh, D, Mosca-Boidron, A-L, Novelli, A, Olivier-Faivre, L, Parker, J, Parker, M J, Patch, C, Pelling, A L, Smol, T, Tümer, Z, Vanakker, O, van Haeringen, A, Vanlerberghe, C, Strydom, A, Skuse, D & Bass, N 2018, ' Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications ', American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, vol. 177, no. 4, pp. 397-405 . https://doi.org/10.1002/ajmg.b.32627
Wolfe, K, McQuillin, A, Alesi, V, Boudry Labis, E, Cutajar, P, Dallapiccola, B, Dentici, M L, Dieux-Coeslier, A, Duban-Bedu, B, Duelund Hjortshøj, T, Goel, H, Loddo, S, Morrogh, D, Mosca-Boidron, A-L, Novelli, A, Olivier-Faivre, L, Parker, J, Parker, M J, Patch, C, Pelling, A L, Smol, T, Tümer, Z, Vanakker, O, van Haeringen, A, Vanlerberghe, C, Strydom, A, Skuse, D & Bass, N 2018, ' Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications ', American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, vol. 177, no. 4, pp. 397-405 . https://doi.org/10.1002/ajmg.b.32627
Recurrent deletions and duplications at the 2q13 locus have been associated with developmental delay (DD) and dysmorphisms. We aimed to undertake detailed clinical characterization of individuals with 2q13 copy number variations (CNVs), with a focus
Autor:
Thygesen, Johan H., Wolfe, Kate, McQuillin, Andrew, Viñas-Jornet, Marina, Baena Díez, Neus, Brison, Nathalie, D'Haenens, Greet, Esteba-Castillo, Susanna, Gabau, Elisabeth, Ribas-Vidal, Núria, Ruiz, Anna, Vermeesch, Joris, Weyts, Eddy, Novell, Ramon, Buggenhout, Griet Van, Strydom, André, Bass, Nicholas, Guitart, Míriam, Vogels, Annick, Universitat Autònoma de Barcelona
Publikováno v:
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
The British Journal of Psychiatry
Thygesen, J H, Wolfe, K, Mcquillin, A, Viñas-jornet, M, Baena, N, Brison, N, D'haenens, G, Esteba-castillo, S, Gabau, E, Ribas-vidal, N, Ruiz, A, Vermeesch, J, Weyts, E, Novell, R, Buggenhout, G V, Strydom, A, Bass, N, Guitart, M & Vogels, A 2018, ' Neurodevelopmental risk copy number variants in adults with intellectual disabilities and comorbid psychiatric disorders ', British Journal of Psychiatry, vol. 212, no. 5, pp. 287-294 . https://doi.org/10.1192/bjp.2017.65
Universitat Autònoma de Barcelona
The British Journal of Psychiatry
Thygesen, J H, Wolfe, K, Mcquillin, A, Viñas-jornet, M, Baena, N, Brison, N, D'haenens, G, Esteba-castillo, S, Gabau, E, Ribas-vidal, N, Ruiz, A, Vermeesch, J, Weyts, E, Novell, R, Buggenhout, G V, Strydom, A, Bass, N, Guitart, M & Vogels, A 2018, ' Neurodevelopmental risk copy number variants in adults with intellectual disabilities and comorbid psychiatric disorders ', British Journal of Psychiatry, vol. 212, no. 5, pp. 287-294 . https://doi.org/10.1192/bjp.2017.65
BackgroundCopy number variants (CNVs) are established risk factors for neurodevelopmental disorders. To date the study of CNVs in psychiatric illness has focused on single disorder populations. The role of CNVs in individuals with intellectual disabi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::982a262f2b96d97559e1406bc3760c5e
https://ddd.uab.cat/record/227912
https://ddd.uab.cat/record/227912
Autor:
Patch, Christine Russell, Wolfe, Kate, Steuber, Kersten, McQuillan, Andrew, Fatima, Jichi, Flinter, Frances, Strydom, Andre, Bass, Nick
Publikováno v:
Patch, C R, Wolfe, K, Steuber, K, McQuillan, A, Fatima, J, Flinter, F, Strydom, A & Bass, N 2017, ' Genetic testing in intellectual disability psychiatry : opinions and practices of UK child and ID psychiatrists ', JOURNAL OF APPLIED RESEARCH IN INTELLECTUAL DISABILITIES . https://doi.org/10.1111/jar.12391
Background: An increasing number of genetic causes of intellectual disabilities (ID) are identifiable by clinical genetic testing, offering the prospect of bespoke patient management. However little is known about the practices of psychiatrists and t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2761::41d718baf96e66252d0f2f18f269e671
https://kclpure.kcl.ac.uk/en/publications/b79fb248-5eb4-4454-851e-140c42920bb3
https://kclpure.kcl.ac.uk/en/publications/b79fb248-5eb4-4454-851e-140c42920bb3
Akademický článek
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Autor:
Wolfe, Kate, Strydom, André, Morrogh, Deborah, Carter, Jennifer, Cutajar, Peter, Eyeoyibo, Mo, Hassiotis, Angela, McCarthy, Jane, Mukherjee, Raja, Paschos, Dimitrios, Perumal, Nagarajan, Read, Stephen, Shankar, Rohit, Sharif, Saif, Thirulokachandran, Suchithra, Thygesen, Johan H, Patch, Christine, Ogilvie, Caroline, Flinter, Frances, McQuillin, Andrew, Bass, Nick
Publikováno v:
Wolfe, K, Strydom, A, Morrogh, D, Carter, J, Cutajar, P, Eyeoyibo, M, Hassiotis, A, McCarthy, J, Mukherjee, R, Paschos, D, Perumal, N, Read, S, Shankar, R, Sharif, S, Thirulokachandran, S, Thygesen, J H, Patch, C, Ogilvie, C, Flinter, F, McQuillin, A & Bass, N 2016, ' Chromosomal microarray testing in adults with intellectual disability presenting with comorbid psychiatric disorders ', European journal of human genetics : EJHG . https://doi.org/10.1038/ejhg.2016.107
European Journal of Human Genetics
European Journal of Human Genetics
Chromosomal copy-number variations (CNVs) are a class of genetic variants highly implicated in the aetiology of neurodevelopmental disorders, including intellectual disabilities (ID), schizophrenia and autism spectrum disorders (ASD). Yet the majorit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::1e1026af462ff904ea409a02a5e5f991
https://kclpure.kcl.ac.uk/en/publications/274e3d50-dcb5-4a4c-bea2-ca6a09c5f75c
https://kclpure.kcl.ac.uk/en/publications/274e3d50-dcb5-4a4c-bea2-ca6a09c5f75c
Autor:
Macri, Diana, Wolfe, Kate
Publikováno v:
Canadian Journal of Dental Hygiene; Jun2019, Vol. 53 Issue 2, p110-117, 8p
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Autor:
Wolfe, Kate, Hilge Thygesen, Johan, McQuillin, Andrew, Viñas-Jornet, Marina, Brison, Nathalie, Esteba-Castillo, Susanna, Ribas-Vidal, Núria, Novell, Ramon, Van Buggenhout, Griet, Strydom, Andre, Bass, Nick, Guitart Feliubadaló, Miriam, Vogels, Annick
Publikováno v:
In European Neuropsychopharmacology 2019 29 Supplement 3:S856-S857